Neuropathology of movement disorders.
暂无分享,去创建一个
[1] K. Jellinger. Pathology of Parkinsonism , 2000, Neurobiology of Aging.
[2] Yaakov Stern,et al. Dementia in Parkinson's disease , 1994, Neurology.
[3] R. Godwin-Austen,et al. Autonomic Failure , 1989 .
[4] W. Gibb,et al. A pathological study of the association between Lewy body disease and Alzheimer's disease. , 1989, Journal of neurology, neurosurgery, and psychiatry.
[5] W. Gibb,et al. Dementia and Parkinson's Disease , 1989, British Journal of Psychiatry.
[6] W. Gibb,et al. THE SIGNIFICANCE OF THE LEWY BODY IN THE DIAGNOSIS OF IDIOPATHIC PARKINSON'S DISEASE , 1989, Neuropathology and applied neurobiology.
[7] M. Piccirilli,et al. Frontal lobe dysfunction in Parkinson's disease: prognostic value for dementia? , 1989, European neurology.
[8] M. Norenberg,et al. Diffuse Lewy body disease and progressive dementia , 1988, Neurology.
[9] W. Gibb,et al. A comparison of clinical and pathological features of young‐ and old‐onset Parkinson's disease , 1988, Neurology.
[10] D. Selkoe,et al. Clinically diagnosed Alzheimer's disease: Autopsy results in 150 cases , 1988, Annals of neurology.
[11] T. Kato,et al. Neurofibrillary tangle formation in the nucleus basalis of meynert ipsilateral to a massive cerebral infarct , 1988, Annals of neurology.
[12] W. Gibb,et al. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease. , 1988, Journal of neurology, neurosurgery, and psychiatry.
[13] S. Carmichael,et al. Decreased catecholamines in the adrenal medulla of patients with parkinsonism. , 1988, The New England journal of medicine.
[14] M. Tennison,et al. Mineralization of the basal ganglia detected by CT in Hallervorden‐Spatz syndrome , 1988, Neurology.
[15] C. Marsden,et al. Pathological report of four patients presenting with cranial dystonias , 1988, Movement disorders : official journal of the Movement Disorder Society.
[16] R. Alberca,et al. Late onset parkinsonian syndrome in Hallervorden-Spatz disease. , 1987, Journal of neurology, neurosurgery, and psychiatry.
[17] W. Gibb,et al. Clinical and pathological features of diffuse cortical Lewy body disease (Lewy body dementia). , 1987, Brain : a journal of neurology.
[18] D. Perl,et al. Adult onset Hallervorden-Spatz disease with neurofibrillary pathology. A discrete clinicopathological entity. , 1987, Brain : a journal of neurology.
[19] L. Kurland,et al. Asymmetric involvement of the spinal cord involving both large and small anterior horn cells in a case of familial amyotrophic lateral sclerosis. , 1987, Clinical neuropathology.
[20] G. Neves,et al. Juvenile Parkinsonism: clinical and metabolic characteristics. , 1987, Journal of neurology, neurosurgery, and psychiatry.
[21] R. Mayeux,et al. Diffuse Lewy body disease. Neuropathological and biochemical studies of six patients. , 1987, Acta neuropathologica.
[22] Niall Quinn,et al. Young onset Parkinson's disease , 1987, Movement disorders : official journal of the Movement Disorder Society.
[23] J. Coyle,et al. Primary Degenerative Dementia Without Alzheimer Pathology , 1986, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.
[24] R. Duvoisin,et al. Hereditary dystonia‐parkinsonism syndrome of juvenile onset , 1986, Neurology.
[25] L. Sternberger,et al. Lewy Body Dementia Without Alzheimer Changes , 1986, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.
[26] W R Gibb,et al. IDIOPATHIC PARKINSON'S DISEASE AND THE LEWY BODY DISORDERS , 1986, Neuropathology and applied neurobiology.
[27] L. Resch,et al. The Nucleus Basalis of Meynert , 1986, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.
[28] J. Mikol,et al. Familial juvenile parkinsonism with multiple systems degenerations A clinicopathological study , 1986, Journal of the Neurological Sciences.
[29] S. Kish,et al. Hallervorden‐Spatz disease: Cysteine accumulation and cysteine dioxygenase deficiency in the globus pallidus , 1985, Annals of neurology.
[30] D. Calne,et al. Dystonia and calcification of the basal ganglia , 1985, Neurology.
[31] Philip J. Langlais,et al. Late‐onset Hallervorden‐Spatz disease presenting as familial parkinsonism , 1985, Neurology.
[32] M. Yokochi,et al. Juvenile parkinsonism--some clinical, pharmacological, and neuropathological aspects. , 1984, Advances in neurology.
[33] P. Averback. TWO NEW LESIONS IN ALZHEIMER'S DISEASE , 1983, The Lancet.
[34] A. Young,et al. New form of familial Parkinson‐dementia syndrome , 1983, Neurology.
[35] C. Ward,et al. Parkinson's disease in 65 pairs of twins and in a set of quadruplets , 1983, Neurology.
[36] K. Shannak,et al. Reversible drug-induced parkinsonism: clinicopathologic study of two cases , 1983 .
[37] G. Serratrice,et al. Chronic spinal muscular atrophy and pallidonigral degeneration , 1983, Neurology.
[38] T. Mizutani,et al. Hereditary multisystemic degeneration with unusual combination of cerebellipetal, dentato-rubral, and nigro-subthalamo-pallidal degenerations. , 1983, Clinical neuropathology.
[39] F. Gabreëls,et al. Progressive idiopathic strio-pallido-dentate calcinosis (Fahr's disease) with autosomal recessive inheritance. Report of three siblings. , 1983, European neurology.
[40] N. Funata,et al. [An autopsy case of Parkinson's disease associated clinically with dementia terminating in akinetic mutism and pathologically with multiple Lewy's Bodies in the cerebral cortex]. , 1982, No to shinkei = Brain and nerve.
[41] J. Hughes. Pathology of amyotrophic lateral sclerosis. , 1982, Advances in neurology.
[42] M. Serdaru,et al. Pallido-luyso-nigral atrophy and amyotrophic lateral sclerosis. , 1981, Acta neuropathologica. Supplementum.
[43] O. Bugiani,et al. Loss of striatal neurons in Parkinson's disease: a cytometric study. , 1980, European neurology.
[44] L. Wolfson,et al. Juvenile parkinsonism: A patient with possible primary striatal dysfunction , 1978, Annals of neurology.
[45] N. Singh,et al. Juvenile parkinsonism treated with levodopa. , 1977, Archives of neurology.
[46] F. Boller,et al. Familial idiopathic cerebral calcifications. , 1977, Journal of neurology, neurosurgery, and psychiatry.
[47] P. Johnson. ANTERIOR HORN CELL EOSINOPHILIC CYTOPLASMIC INCLUSION BODIES IN SPORATIC MOTOR NEURON DISEASE OF ADULTS: 137 , 1976 .
[48] G. Horowitz,et al. Pallido-pyramidal syndrome treated with levodopa. , 1975, Journal of neurology, neurosurgery, and psychiatry.
[49] James M. Powers,et al. Wetherbee Ail , 1974, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.
[50] K. Jellinger,et al. Brain dopamine and the syndromes of Parkinson and Huntington. Clinical, morphological and neurochemical correlations. , 1973, Journal of the neurological sciences.
[51] U. Roessmann,et al. Familial striatal degeneration. , 1973, Archives of neurology.
[52] Y. Yamamura,et al. Paralysis agitans of early onset with marked diurnal fluctuation of symptoms , 1973, Neurology.
[53] K. Kosaka,et al. [An autopsy case of unclassifiable presenile dementia]. , 1973, Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica.
[54] K. Jellinger,et al. Neuroaxonal dystrophy in man: character and natural history. , 1971, Acta neuropathologica.
[55] J. Resch,et al. Juvenile parkinsonism. , 1971, Archives of neurology.
[56] E. Christensen,et al. NEUROPATHOLOGICAL INVESTIGATION OF 28 BRAINS FROM PATIENTS WITH DYSKINESIA , 1970, Acta psychiatrica Scandinavica.
[57] E. Lange,et al. Familial progressive pallidum atrophy. , 1970, European neurology.
[58] L. Forno,et al. CONCENTRIC HYALIN INTRANEURONAL INCLUSIONS OF LEWY TYPE IN THE BRAINS OF ELDERLY PERSONS (50 INCIDENTAL CASES): RELATIONSHIP TO PARKINSONISM , 1969, Journal of the American Geriatrics Society.
[59] M. A. Neumann. A comparative study of Parkinsonism and other extrapyramidal system disorders. , 1968, Journal of neuropathology and experimental neurology.
[60] E. Richardson,et al. Corticodentatonigral degeneration with neuronal achromasia. , 1968, Archives of neurology.
[61] K. Jellinger,et al. ["Striato-nigral degeneration"]. , 1968, Acta neuropathologica.
[62] W. Mccormick,et al. Familial degeneration of the pallidonigral system , 1965, Neurology.
[63] H. Pakkenberg. GLOBUS PALLIDUS IN PARKINSONISM , 1963, Acta neurologica Scandinavica. Supplementum.
[64] K. Tamura,et al. [An autopsy case of Parkinson's disease]. , 1962, No to shinkei = Brain and nerve.
[65] G. Spellman. Report of familial cases of parkinsonism. Evidence of a dominant trait in a patient's family. , 1962, JAMA.
[66] L. Lipkin,et al. DIFFUSE INTRACYTOPLASMIC GANGLIONIC INCLUSIONS (LEWY TYPE) ASSOCIATED WITH PROGRESSIVE DEMENTIA AND QUADRIPARESIS IN FLEXION , 1961, Journal of neuropathology and experimental neurology.
[67] L. Lipkin. Cytoplasmic inclusions in ganglion cells associated with parkinsonian states: a neurocellular change studied in 53 cases and 206 controls. , 1959, The American journal of pathology.
[68] O. Ueda,et al. Familial paralysis agitans juvenilis; a clinical, anatomical and genetic study. , 1958, Folia psychiatrica et neurologica japonica.
[69] J. F. Martin,et al. Symmetrical calcification of the basal ganglia with familial ataxia and pigmentary macular degeneration. , 1957, Brain : a journal of neurology.
[70] W. Hawke,et al. BILATERAL SYMMETRICAL NECROSIS OF THE CORPORA STRIATA: Report of a Fatal Case and Reference to a Possible Syndrome of the Corpora Striata , 1951, The Journal of nervous and mental disease.
[71] F. Mettler. Fiber connections of the corpus striatum of the monkey and baboon , 1945 .
[72] J. Hunt. Progressive atrophy of the globus pallidus (primary atrophy of the pallidal system). A system disease of the paralysis agitans type, characterized by atrophy of the motor cells of the corpus striatum. A contribution to the functions of the corpus striatum , 1917 .
[73] J. Bury. TWO CASES OF PARALYSIS AGITANS IN THE SAME FAMILY, IN WHICH IMPROVEMENT FOLLOWED THE ADMINISTRATION OF HYOSCINE. , 1902 .